SLC10A2

solute carrier family 10 member 2
OMIM: 601295, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red SLC10A2 in Neonatal cholestasis

Level 3: Liver disease
Level 2: Gastroenterological disorders
Version 1.26

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Emory Genetics Laboratory
Phenotypes
  • Bile acid malabsorption, primary 613291
Green SLC10A2 in Intestinal failure or congenital diarrhoea


Version 3.3
Latest signed off version: v3.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • ?Bile acid malabsorption, primary, 1, OMIM:613291